chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
17
40132773
40132774
A
C
16
GENIC
homozygous
140114862
17
40133388
40133389
G
A
20
GENIC
homozygous
140114863
17
40133840
40133841
A
G
24
GENIC
homozygous
140114864
17
40133903
40134016
ATTGGACTACAGGGAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAGAACCAAAAAAA
17
GENIC
homozygous
140022386
17
40134775
40134776
A
C
27
GENIC
homozygous
140114865
17
40135831
40135832
A
G
12
GENIC
homozygous
140114866
17
40136302
40136303
G
A
16
GENIC
homozygous
140114867
17
40136472
40136473
A
G
19
GENIC
homozygous
140114868
17
40137247
40137248
T
C
20
GENIC
homozygous
140114869
17
40137821
40137822
A
G
26
GENIC
homozygous
140114870
17
40138435
40138436
C
T
16
GENIC
homozygous
140114871
17
40139133
40139134
A
G
15
GENIC
homozygous
140114872
17
40139218
40139218
C
15
GENIC
homozygous
140022387
17
40140780
40140781
G
T
26
GENIC
homozygous
140114873
17
40142462
40142463
C
T
25
GENIC
homozygous
140114874
17
40142877
40142878
T
C
19
GENIC
homozygous
140114875
17
40145002
40145003
A
G
21
GENIC
homozygous
140114876
17
40145250
40145251
G
A
24
GENIC
homozygous
140114877
17
40145349
40145350
G
A
24
GENIC
homozygous
140114878
17
40148699
40148700
T
C
23
GENIC
homozygous
140114879
17
40150210
40150211
G
A
19
GENIC
homozygous
140114880
17
40151433
40151434
T
C
15
GENIC
homozygous
140114881
17
40154752
40154753
C
G
28
GENIC
homozygous
140114882
17
40155687
40155688
C
T
34
GENIC
homozygous
140114883
17
40156777
40156778
A
G
27
GENIC
homozygous
140114884
17
40157038
40157038
TCTGAAAATAAGCATTTT
11
GENIC
homozygous
140022388
17
40157151
40157151
T
31
GENIC
possibly homozygous
140022389
17
40158589
40158590
T
G
19
GENIC
homozygous
140114885
